Elevation in white blood cell count and development of hyper LDL cholesterolemia

To investigate the relationship between white blood cell (WBC) count and incidence of hyper-low-density lipoprotein (LDL) cholesterolemia in a population-based longitudinal study. This is a retrospective study using data of annual health check-ups for residents of Iki City, Japan. A total of 3312 residents (≥ 30 years) without hyper-LDL cholesterolemia at baseline were included in this analysis. Primary outcome was incidence of hyper-LDL cholesterolemia (LDL cholesterol levels ≥ 3.62 mmol/L and/or use of lipid lowering drugs). During follow-up (average 4.6 years), 698 participants development of hyper-LDL cholesterolemia (incidence 46.8 per 1000 person-years). Higher incidence of hyper-LDL cholesterolemia was observed among participants with higher leukocyte count (1st quartile group: 38.5, 2nd quartile group: 47.7, 3rd quartile group: 47.3, and 4th quartile group: 52.4 per 1,000 person-years, P = 0.012 for trend). Statistically significant relation was observed even after adjustment for age, gender, smoking, alcohol intake, leisure-time exercise, obesity, hypertension and diabetes: hazard ratio 1.24 (95% confidence interval 0.99 to 1.54) for 2nd quartile group, 1.29 (1.03–1.62) for 3rd quartile group and 1.39 (1.10–1.75) for 4th quartile group, compared with 1st quartile group (P for trend = 0.006). Increased WBC count was related to incidence of hyper-LDL cholesterolemia in general Japanese population.

Data collection. At baseline, casual blood samples were collected. All blood tests were conducted measured in a single laboratory (CRC Co., Ltd., Fukuoka, Japan) using standardized procedures throughout the study period. The WBC count was obtained using an automatic blood cell calculator (XN-1000®; Sysmex Corporation, Kobe, Japan). Participants were categorized into 4 groups using quartiles of the leucocyte count: quartile 1 (< 4400/μL), quartile 2 (4400-5300/μL), quartile 3 (5400-6500/μL), and quartile 4 (6500/μL <). Serum LDL cholesterol, High-density lipoprotein (HDL) cholesterol and triglyceride (TG) levels were estimated enzymatically. Plasma glucose concentrations were also estimated enzymatically. HbA1c levels (NGSP [National Glycohemoglobin Standardization Program] value) were estimated using HPLC (high-performance liquid chromatography) method. The presence of diabetes was defined by glucose concentration in fasting status ≥ 7.0 mmol/L, glucose concentration in non-fasting status ≥ 11.1 mmol/L, HbA1c ≥ 6.5%, and/or the use of glucose lowering treatment 13 . Information on smoking, daily alcohol intake, regular exercise habits, and use of medications was obtained using standardized questionnaire. Current smokers were defined as residents who had smoked continuously for more than 6 months or those who had smoked more than one-hundred cigarettes at baseline. Definition of outcome. During the study period between 2008 and 2017, the first visit of the health examination for each participant was defined as baseline examination. Participants were followed-up to the last visit of the follow-up health examination. The endpoint was incidence of hyper-LDL cholesterolemia (elevation of LDL cholesterol level to ≥ 3.62 mmol/L and/or initiation of lipid lowering agents during follow-up) 17 . Participants whose LDL cholesterol levels returned to < 3.62 mmol/L without lipid lowering agents at the last follow-up visit were not regarded as incident hyper-LDL cholesterolemia. We have also conducted sensitivity analysis defining the first time diagnosed with hyper-LDL cholesterolemia as incidence.

Statistical analysis.
Continuous characteristic values were shown as mean ± SD, and p values for trend across WBC count groups were estimated with use of simple regression models. Categorical characteristic variables were shown as participant number (%), and p values for trends across WBC count groups were estimated with use of logistic regression models. With regard to incidence of hyper-LDL cholesterolemia in each WBC group, the person-year method was used. The association between WBC count groups and incidence of hyper-LDL cholesterolemia was investigated using Cox's proportional hazards analysis, and the effects of WBC count were reported using hazard ratios (HRs) and 95% confidence intervals (95% CIs). Proportional hazards assumption was assessed using cumulative sums of martingale-based residuals and using Schoenfeld residuals 18 . Multivariable-adjusted Cox's proportional hazards included age, gender, current smoking habits, current alcohol intake, exercise habits, obesity, hypertension, and diabetes as covariates. P values for trend across 4 groups of WBC count were obtained from tests for the presence of an association between an ordinal variable of WBC count with 4 categories and the outcome using Cox's proportional hazards models. Subgroup analyses were conducted according to other risk factors such as age, gender, smoking, exercise, obesity, diabetes, and the differences in the associations between WBC count and incidence of the outcome between subgroups were tested by adding an interaction term to the statistical model. P < 0.05 was considered statistically significant. SAS version 9.4 was used for the statistical analysis of the paper.

Results
Baseline characteristics by quartiles of leucocyte count were shown in Table 1. Higher leucocyte counts were associated with younger age and male gender. Participants with higher leucocyte counts were more likely to be current smokers, current drinkers, obese, hypertensive and diabetic. During 4.6 years of mean follow-up, incidence of hyper-LDL cholesterolemia was observed among 698 participants (incidence 46.8/1000 person-years). Table 2 shows the association between leucocyte count and incidence of hyper-LDL cholesterolemia. The annual incidence of hyper-LDL cholesterolemia increased with elevation of the WBC count (38. 5 Table 1). Table 3 shows the association between quartiles of white blood cell count and hyper-low-density lipoprotein cholesterolemia in subgroups. Comparable effects of leucocyte count for incidence of hyper-LDL cholesterolemia were observed between subgroups defined by age (< 65 vs. ≥ 65 years), gender, smoking, exercise, obesity, and diabetes (all p interaction > 0.1).

Discussion
In our study, we found that there was a statistically significant relationship between the increase in WBC count and future development of hyper-LDL cholesterolemia in general Japanese men and women. This result was also statistically significant after adjusting for age, gender, smoking, drinking, regular exercise, obesity, hypertension, and diabetes. There were also comparable associations between subgroups defined by age, gender, smoking, exercise, obesity, and diabetes.
There are several reports from observational studies which reported the association between white blood cell count and hyper-LDL cholesterolemia. In a cross-sectional study of 10,866 Chinese hypertensive populations, there was a positive correlation between WBC count and serum LDL cholesterol with or without diabetes 7 . At a health care center of a hospital, 2588 Japanese health checkup participants were followed for 4 years, and lymphocyte counts were significantly positively correlated with incidence of hyper-LDL cholesterolemia 6 . In the present long-term, large-scale observational study of general Japanese confirmed the results of the prior studies and have shown that increase in WBC count was associated with future incidence of hyper-LDL cholesterolemia.
Current evidence of the association between WBC count and LDL cholesterol has been mainly derived from Asia (including Japan) 6,7,19 . This fact might in part be attributable to lower levels of inflammatory markers in Asian people 20 , whose dietary pattern is correlated with higher consumption of soybean products, fish, seaweeds, vegetables, fruits and green tea and with lower consumption of meat and fat 21 , than those in Western people. www.nature.com/scientificreports/ Future research to compare the associations between WBC count and LDL cholesterol across different regions is required to confirm possible regional heterogeneity.
Smoking is a possibly important confounding factor in the present analysis because WBC count is strongly associated with current smoking status 22 . In the present analysis, however, there were no clear evidence of interaction between WBC count and current smoking for incidence of hyper-LDL cholesterolemia (P = 0.90 for interaction). Furthermore, in multivariable analysis, the association between WBC count and incidence of hyper-LDL cholesterolemia was independent of other confounding factors including current smoking. Therefore, the relationship between WBC count and hyper-LDL cholesterolemia seems to be independent of possible confounding effects of smoking.
The mechanism of the link between elevated leukocyte count and hyper-LDL cholesterolemia have not been clarified, but the following hypothesis is conceivable. Elevation of leukocytes is likely to represent inflammatory reaction in adipose tissue associated with visceral fat accumulation [23][24][25][26] , which has been shown to cause insulin resistance. Insulin resistance has been shown to elevate LDL-cholesterol levels through pool of LDL precursors including very-low-density lipoprotein (VLDL) due to increased production and decreased clearance associated with decreased activity of lipoprotein lipase (LPL) 27,28 . More specifically, insulin resistance has been shown to reduce inhibition of hormone-sensitive lipase in adipose tissue by hyperinsulinemia and increased free fatty acid (FFA) level in hepatocyte 27,28 . Elevated of FFA has been shown to reduce in degradation of apo B in hepatocytes 27,28 . It also suppresses phosphoinositide (PI) 3-kinase mediated apoB degradation and accelerates the action of microsomal triglyceride transfer protein (MTP), a rate-limiting factor of VLDL assembly 27,28 . Moreover, TG-riched and enlarged VLDL1 has been shown to increase by increased activity of two factors involved in the formation of VLDL 1 : phospholipase D1 and ADP ribosylation factor 1 (ARF-1) 27 . Insulin resistance is also likely to increase circulated LDL through LDL receptor (LDLR) degradation due to upregulated hepatic lipase levels and decreased LDLR binding ability due to increase in oxidized, saccharified or small-dense LDL 27,29 . Smalldens LDL has been shown to be created by increased activity of Cholesteryl ester transfer protein (CETP), which Table 3. Association between quartiles of white blood cell count and hyper-low-density lipoprotein cholesterolemia in subgroups. *Adjusted for age (except for subgroup analysis by age), sex (except for subgroup analysis by sex), smoking, exercise, obesity (except for subgroup analysis by obesity), and diabetes. www.nature.com/scientificreports/ transfer TGs from TG-rich lipoproteins to LDL, and hepatic triglyceride lipase 27,28 . Furthermore, hepatic insulin resistance appears to increase proprotein convertase subtilisin/kexin type 9 (PCSK9) levels, which promotes degradation and reduction of LDLR and subsequent increase in LDL 29,30 . This study has several limitations. First, because this was a retrospective cohort study with irregular visits for some participants, the actual data of the new onset of hyper-LDL cholesterolemia was not clear. Next, healthconscious people were more likely to have visited health examinations and were more likely to have been included in the analysis than residents with unhealthy lifestyle. Third, we have no information on WBC fraction such as neutrophil count, neutrophil/lymphocyte ratio etc., and other inflammatory marker such as C reactive protein, TNF-α, IL-1β etc. Fourth, we do not have information on co morbidities (such as infection, cancer, leukemia etc.) which might affect WBC counts. Fifth, we have missing information on nutritional factors.

Conclusion
In the general population of Japanese adults, increase in leukocyte count was related to future development of hyper-LDL cholesterolemia. In addition to management of traditional cardiovascular risk factors, high-risk approach based on WBC count might add further protection against the future onset of hyper-LDL cholesterolemia and subsequent cardiovascular events/mortality.

Data availability
The datasets generated and/or analysed during the current study are not publicly available due to the property of the Iki CIty, Nagasaki, Japan and cannot be made public as it may result in violation of the Act on the Protection of Personal Information of the Japanese government but are available from the corresponding author on reasonable request.